- Solvent and acid/base chemistry
- Prebiotic carbon/nitrogen compounds

Rule-derived, not scripted
The simulation begins with chemistry, matter, energy, and environmental gradients. It starts with no distinction between living and nonliving — everything in it consists of chemicals interacting under the same rules.
Organized systems appear only because the underlying physical and chemical rules make them possible. Nothing is granted organism-like status; it is earned as an observed behaviour, or it is not there at all.
Intended causal chain
The chain proceeds only if the simulated conditions allow those things to occur. Each arrow is conditional, never scheduled.
Properties that must be observed (12)
Binding constraints
Run context
Elapsed simulated time41.7 h simulatedadvancing
Thioester coupling sustaining the acetyl-thioester network.

Begin with chemistry, matter, energy and environmental gradients. Organized systems appear only if the underlying physical and chemical rules make them possible.
Begin the experimentThe Ultimate Experiment
Built for the people who ask it. A laboratory instrument for
It begins with chemistry, matter, energy, and environmental gradients — and nothing else. No outcome is authored ahead of the run. The central rule governs everything downstream: Script the laws. Do not script life. A single instruction is deliberately missing from the source — spawnLife() does not exist.
Causal chain
This is the sequence the simulation is permitted to traverse. Each stage is a consequence of the one before it, computed from the rules rather than issued as an instruction.
The chain proceeds only if the simulated conditions allow those things to occur. No stage is scheduled, guaranteed, or triggered by a named life event.
Matter, energy and environmental gradients set the arena; no outcome beyond these laws is prescribed.
Bond formation and acid/base equilibria proceed from energetics and rates alone.
Coupling between reactions yields networks whose structure was never enumerated in advance.
Local order appears where flux, catalysis and surface chemistry make it favourable.
Amphiphile self-assembly produces boundaries that concentrate their own contents.
Products that catalyse further product formation can propagate when kinetics allow.
Imperfect copying and side reactions generate a spread of descendant compositions.
Whatever persists longest and multiplies fastest dominates the population by physics, not by scoring.
Composition drifts and accumulates across generations; nothing is directed toward a target form.
Physics → chemistry → reaction networks → self-organization → compartments → replication → variation → differential persistence → evolution.
Every stage after the first is written as conditional, because the laws decide.
Initial Inventory
Every species below enters the same kinetic reaction network. None of them is a collectible resource, a label for life, or a privileged ancestor — they are simply matter and energy under the same rules as everything that follows.
13 classes126 species
Water is modelled as the bulk solvent at the continuum level; local pH emerges from acid/base concentrations. Individual water molecules are not rendered.
Concentrations feed ionic strength, membrane stability, polymer folding, precipitation and reaction rates.
Gas exchange between atmosphere and water follows solubility and partial pressure.
Kinetic network participants, not collectible resources.
Additional carboxylic acids may emerge from valid transformations.
Condensation into short peptides only — no modern protein synthesis is assumed.
Instability and degradation are included; ribose is not immortal.
Thymine may arise later but need not dominate primordial chemistry.
ADP and ATP are possible products of chemistry, never supplied as a universal primordial energy currency.
Phosphate adsorption to minerals and the realistic difficulty of phosphorylation are modelled.
Thioester chemistry couples energetically favourable and unfavourable reactions.
Amphiphilic behaviour arises from molecular structure — above threshold concentration these species self-assemble.
Surfaces enter here as inventory only; adsorption, catalysis and phosphate binding are treated in the mineral band.
Starting chemistry, not the universe
This library is the starting chemistry, not the universe of possible chemistry. Species that were never listed are constructed dynamically from valid chemical transformations, each new molecule carrying the same grammar of properties as the ones above.
The mineral world13 surfaces
Every reaction below runs against a mineral interface. Each surface contributes a distinct physical role — adsorption, catalysis, phosphate retention, redox mediation — and the same ledger governs both the dissolved species and the surfaces they touch.
Reduced-iron sulfide surface that binds dissolved metals and hosts early thioester-forming chemistry.
Persistent sulfide mineral whose surface couples electron transfer and drives reductive carbon fixation.
Mixed-valence sulfide offering both electron donors and acceptors at the same interface.
Nickel sulfide surface that adsorbs cyanide species and catalyses their condensation.
Mixed ferrous–ferric oxide that adsorbs organics and mediates redox gradients.
Mineral framework providing high-surface-area scaffolding for concentrating dilute organics.
Hydration product of olivine; its formation releases hydrogen and drives alkaline vent chemistry.
Primary mantle silicate whose aqueous alteration supplies the reducing power of serpentinizing systems.
Alkaline hydroxide layer that buffers local pH and stabilises anionic intermediates.
Precipitating carbonate phases that fix dissolved CO₂ and regulate alkalinity.
Ferric oxide phases that adsorb phosphate and anionic species onto their surfaces.
Swelling clay whose interlayer cations adsorb nucleotides and template polymer condensation.
Phosphate-bearing surfaces that adsorb orthophosphate and make phosphorylation energetically reachable.
Boundary condition
No mineral surface here is granted behaviour the chemistry does not give it — the surfaces are laws, not actors.
Adsorption affinities, catalytic groups and phosphate binding are properties of the mineral, evaluated per collision like every dissolved species. Nothing is placed by hand at the interface.
Above the concentration where packing beats dissolution, amphiphiles assemble the same way the bulk solvent pushes them to — into micelles, sheets, droplets and vesicles. No cell membrane object is scripted first: a membrane is a consequence of molecular structure and local concentration, and it keeps changing for as long as the chemistry around it does.
C8–C18 amphiphile aggregate
Above the critical aggregate concentration, amphiphile tails sequester from water and heads face the bulk solvent, closing into a spherical aggregate with no interior volume.
spherical aggregateplanar bilayer lamella
At lower curvature the same molecules pack into extended lamellae. Sheets stack, slide against one another and expose mineral surfaces to a two-dimensional reaction field.
extended bilayersurfactant-stabilised organic phase
A sparingly soluble organic phase is stabilised by an adsorbed amphiphile monolayer, creating a bounded interior without any pre-declared boundary object.
soft interfaceclosed bilayer compartment
When a sheet closes on itself it encloses a volume of bulk solution. The boundary is a thin refractive shell a few nanometres thick, assembled entirely by the packing of its amphiphiles.
closed aqueous compartmentAmphiphiles exchange from solution into an existing boundary faster than they leave it, so the structure gains area.
When the local amphiphile concentration falls below equilibrium, the reverse flux dominates and the structure loses molecules.
Two boundaries that meet can merge into a single larger structure, combining their enclosed volumes and contents.
A destabilised boundary fails, releases its contents to the bulk solution, and its amphiphiles return to the free pool.
There is no cell membrane object in the model. No compartment is declared, labelled, or given a lifetime by the program — a boundary exists only while amphiphile flux keeps it closed.
A membrane originates from amphiphile self-assembly. Compartments appear only where the simulated concentration, temperature and ionic conditions make closure favourable, and they persist only while that remains true.
Each category below is an outcome the model is permitted to reach, never an instruction it is given. Nothing was explicitly told the program to make. Every marker on this axis is a chemical consequence of the laws set upstream, not a run history. Outcomes can be inspected in the Emergence and Structures surfaces.
Possible outcome
conditional on chemistry
Autocatalytic networks may persist
Persistence · 01
reaction cycles sustained while the gradient holds
Possible outcome
conditional on chemistry
Compartments may self-assemble
Persistence · 02
boundaries persist while amphiphile supply continues
Possible outcome
conditional on chemistry
Templated copying appears
Persistence · 03
copy lineages persist only as long as their chemistry is resupplied
Possible outcome
conditional on chemistry
Imperfect descendants accumulate
Persistence · 04
variant populations persist where their kinetics permit
Possible outcome
conditional on chemistry
Some lineages outlast others
Persistence · 05
persisting lineages outlast non-persisting ones
Nothing was told to appear
There is no spawn command in this model, and no branch that rewards one molecule over another. A structure held together here because its chemistry let it hold together — a marker on the axis is a consequence, not an event trigger.
Where to watch it happen
The same quantities tracked along this axis resolve into the Emergence surface, where autocatalytic sets and compartments can be tracked if they form, and into the Structures surface, which holds the assembled forms and their persistence over simulated time.
No comments yet. Be the first!